Prolonged Xenograft Survival Induced by Inducible Costimulator-Ig is Associated With Increased Forkhead Box P3+ Cells
| dc.contributor.author | Hodgson, Russell | |
| dc.contributor.author | Christiansen, Dale | |
| dc.contributor.author | Ziolkowski, Andrew | |
| dc.contributor.author | Mouhtouris, Effie | |
| dc.contributor.author | Simeonovic, Charmaine | |
| dc.contributor.author | Ierino, Francesco | |
| dc.contributor.author | Sandrin, Mauro | |
| dc.date.accessioned | 2015-12-10T23:32:44Z | |
| dc.date.issued | 2011 | |
| dc.date.updated | 2016-02-24T08:19:01Z | |
| dc.description.abstract | Background: Blockade of the inducible costimulator (ICOS) pathway has been shown to prolong allograft survival; however, its utility in xenotransplantation is unknown. We hypothesize that local expression of ICOS-Ig by the xenograft will suppress the T-cell response resulting in significant prolonged graft survival. METHODS.: Pig iliac artery endothelial cells (PIEC) secreting ICOS-Ig were generated and examined for the following: (1) inhibition of allogeneic and xenogeneic proliferation of primed T cells in vitro and (2) prolongation of xenograft survival in vivo. Grafts were examined for Tregs by flow cytometry and cytokine levels determined by quantitative reverse-transcriptase polymerase chain reaction. Results: Soluble ICOS-Ig markedly decreased allogeneic and xenogeneic primed T-cell proliferation in a dose-dependent manner. PIEC-ICOS-Ig grafts were significantly prolonged compared with wild-type grafts (median survival, 34 and 12 days, respectively) with 20% of PIEC-ICOS-Ig grafts surviving more than 170 days. Histological examination showed a perigraft cellular accumulation of Forkhead box P3 (Foxp3) cells in the PIEC-ICOS-Ig grafts, these were also shown to be CD3+CD4+CD25+. Survival of wild-type PIEC grafts in a recipient simultaneously transplanted with PIEC-ICOS-Ig were also prolonged, with a similar accumulation of Foxp3 cells at the periphery of the graft demonstrating ICOS-Ig induces systemic graft prolongation. However, this prolongation was specific for the priming xenograft. Intragraft cytokine analysis showed an increase in interleukin-10 levels, suggesting a potential role in induction/function of CD4+CD25+Foxp3+ cells. Conclusions: This study demonstrates prolonged xenograft survival by local expression of ICOS-Ig, we propose that the accumulation of CD4+CD25+Foxp3+ cells at the periphery of the graft and secretion of interleukin-10 is responsible for this novel observation. | |
| dc.identifier.issn | 0041-1337 | |
| dc.identifier.uri | http://hdl.handle.net/1885/68968 | |
| dc.publisher | Lippincott Williams & Wilkins | |
| dc.source | Transplantation | |
| dc.subject | Keywords: CD28 antigen; complementary DNA; cytotoxic T lymphocyte antigen 4; immunoglobulin; immunoglobulin Fc fragment; inducible costimulator; interleukin 10; transcription factor FOXP3; unclassified drug; animal cell; animal experiment; animal model; article; CD Foxp3; ICOS-Ig; Treg; Xenotransplantation | |
| dc.title | Prolonged Xenograft Survival Induced by Inducible Costimulator-Ig is Associated With Increased Forkhead Box P3+ Cells | |
| dc.type | Journal article | |
| local.bibliographicCitation.issue | 10 | |
| local.bibliographicCitation.lastpage | 1097 | |
| local.bibliographicCitation.startpage | 1090 | |
| local.contributor.affiliation | Hodgson, Russell, University of Melbourne and Austin Health | |
| local.contributor.affiliation | Christiansen, Dale, Austin Health and University of Melbourne | |
| local.contributor.affiliation | Ziolkowski, Andrew, College of Medicine, Biology and Environment, ANU | |
| local.contributor.affiliation | Mouhtouris, Effie, University of Melbourne and Austin Health | |
| local.contributor.affiliation | Simeonovic, Charmaine, College of Medicine, Biology and Environment, ANU | |
| local.contributor.affiliation | Ierino, Francesco, Austin Research Institute | |
| local.contributor.affiliation | Sandrin, Mauro, Austin Research Institute | |
| local.contributor.authoruid | Ziolkowski, Andrew, u3292935 | |
| local.contributor.authoruid | Simeonovic, Charmaine, u8205698 | |
| local.description.embargo | 2037-12-31 | |
| local.description.notes | Imported from ARIES | |
| local.identifier.absfor | 110708 - Transplantation Immunology | |
| local.identifier.absseo | 920108 - Immune System and Allergy | |
| local.identifier.ariespublication | f2965xPUB1881 | |
| local.identifier.citationvolume | 91 | |
| local.identifier.doi | 10.1097/TP.0b013e31821774e0 | |
| local.identifier.scopusID | 2-s2.0-79955591494 | |
| local.identifier.thomsonID | 000290208500009 | |
| local.type.status | Published Version |
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